Newsroom

Insights and information on our approach to raising awareness of rare diseases, developing new therapies, and supporting our team.

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Living with ABCC6 Deficiency

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Investigational Therapy INZ-701 for ENPP1 Deficiency

CheckRare - Madaline Spencer

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ENPP1 and ABCC6 Deficiency Data Presented at ASBMR 2024

CheckRare: ENPP1 and ABCC6 Deficiency Data Presented at ASBMR 2024 - Madaline Spencer

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US FDA’s Rare Pediatric Voucher Program Faces Tight Deadline For Reauthorization

Pink Sheet - Sue Sutter

Newsroom thumbnail for Matt Wintons article on BioSpace

Opinion: Congress Must Reauthorize FDA Program for Pediatric Rare Diseases

BioSpace - Matthew Winton

Check Rare Poster

Clinical Trial for ENPP1 and ABCC6 Deficiency

Check Rare - Doug Treco

Check Rare Poster

ENPP1 and ABCC6 Deficiency Overview

Check Rare - Doug Treco

The Power and Potential of GACI Clinical Trials

Figure1 - Podcast Season 10, Episode 2

INZ-701 Trial Update – 2024 PXE Extended Virtual Conference

PXE International - Interview with Yves Sabbagh

State of the Orphan Space

Life Science Leader - Doug Treco Interview

Facilitating Newborn Screening and Early Intervention for Infants Born with Rare Diseases

Catherine Nester byline – Page 25

ENPP1 Deficiency Disorders with Inozyme

DNA Today Podcast - Interview with Yves Sabbagh and Christine O’Brien

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The Inozyme Advocate

Rare Community Profiles: Inozyme’s Catherine Nester Discusses Newborn Screening and the GACI Diagnostic Delay

Catherine Nester Interview

Catherine Nester Discusses the BeginNGS Tool for Newborn Rare Disease Screening Awareness

Catherine Nester Interview

Rady Children’s Institute for Genomic Medicine Launches Phase 2 of BeginNGS Program for Identifying Treatable Genetic Diseases for Newborns

Rady Children’s Press Release

Check Rare Poster

What is ENPP1 Deficiency?

Check Rare - Catherine Nester Interview

Check Rare Poster

The Prevalence of ENPP1 Deficiency

Check Rare - Catherine Nester and Mark Kiel Interview

Dr. Yves Sabbagh – Update on INZ-701 Trial for PXE-2023 – PXE Global Conference

PXE International - Interview with Yves Sabbagh

Hypophosphatemia and the Secret Locked in a Child’s DNA

Figure1 - Podcast Season 6, Episode 3

Mysterious Arterial Calcifications and One of the World’s Most Unique Patients

Figure1 - Podcast Season 6, Episode 1

Rare Disease Report Podcast: Newborn Screening Awareness and Novel Diagnostic Tool

HCP Live – Rare Disease Report Podcast - Interview with Catherine Nester and Dr. Stephen Kingsmore

Wait, How Do You Spell That? A Rare Disease Podcast

GACI Global and Catherine Nester Interview

Advancing Newborn Screening Toward Improving Pediatric Rare Genetic Diseases

Today’s Clinical Lab – Podcast - Interview with Catherine Nester

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Dr. Gary Zammit speaks with Catherine Nester of Inozyme about clinical trials in rare disease

The earlier the better: New consortium leverages infant screening to accelerate treatment

Catherine Nester and Dr. Stephen Kingsmore Interview

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The Inozyme Advocate

The Inozyme Advocate

The Inozyme Advocate

The Inozyme Advocate

The Inozyme Advocate